Modelling neurodegeneration in Saccharomyces cerevisiae: why cook with baker's yeast?

V Khurana, S Lindquist - Nature Reviews Neuroscience, 2010 - nature.com
In ageing populations, neurodegenerative diseases increase in prevalence, exacting an
enormous toll on individuals and their communities. Multiple complementary experimental …

Replicative aging in yeast: the means to the end

KA Steinkraus, M Kaeberlein… - Annual review of cell …, 2008 - annualreviews.org
Progress in aging research is now rapid, and surprisingly, studies in a single-celled
eukaryote are a driving force. The genetic modulators of replicative life span in yeast are …

[HTML][HTML] A liquid to solid phase transition underlying pathological huntingtin exon1 aggregation

TR Peskett, F Rau, J O'Driscoll, R Patani, AR Lowe… - Molecular cell, 2018 - cell.com
Huntington's disease is caused by an abnormally long polyglutamine tract in the huntingtin
protein. This leads to the generation and deposition of N-terminal exon1 fragments of the …

Misfolded proteins partition between two distinct quality control compartments

D Kaganovich, R Kopito, J Frydman - Nature, 2008 - nature.com
The accumulation of misfolded proteins in intracellular amyloid inclusions, typical of many
neurodegenerative disorders including Huntington's and prion disease, is thought to occur …

[HTML][HTML] Chapter 4: Protein interactions and disease

MW Gonzalez, MG Kann - PLoS computational biology, 2012 - journals.plos.org
Proteins do not function in isolation; it is their interactions with one another and also with
other molecules (eg DNA, RNA) that mediate metabolic and signaling pathways, cellular …

A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity

BS Johnson, JM McCaffery… - Proceedings of the …, 2008 - National Acad Sciences
Protein misfolding is intimately associated with devastating human neurodegenerative
diseases, including Alzheimer's, Huntington's, and Parkinson's. Although disparate in their …

Yeast reveal a “druggable” Rsp5/Nedd4 network that ameliorates α-synuclein toxicity in neurons

DF Tardiff, NT Jui, V Khurana, MA Tambe… - Science, 2013 - science.org
α-Synuclein (α-syn) is a small lipid-binding protein implicated in several neurodegenerative
diseases, including Parkinson's disease, whose pathobiology is conserved from yeast to …

Impaired ERAD and ER stress are early and specific events in polyglutamine toxicity

ML Duennwald, S Lindquist - Genes & development, 2008 - genesdev.cshlp.org
Protein misfolding, whether caused by aging, environmental factors, or genetic mutations, is
a common basis for neurodegenerative diseases. The misfolding of proteins with abnormally …

The pathobiology of perturbed mutant huntingtin protein–protein interactions in Huntington's disease

EE Wanker, A Ast, F Schindler, P Trepte… - Journal of …, 2019 - Wiley Online Library
Mutations are at the root of many human diseases. Still, we largely do not exactly
understand how they trigger pathogenesis. One, more recent, hypothesis has been that they …

[HTML][HTML] Target-based discovery of an inhibitor of the regulatory phosphatase PPP1R15B

A Krzyzosiak, A Sigurdardottir, L Luh, M Carrara, I Das… - Cell, 2018 - cell.com
Protein phosphorylation is a prevalent and ubiquitous mechanism of regulation. Kinases are
popular drug targets, but identifying selective phosphatase inhibitors has been challenging …